4.3 Article

miR-382 targeting PTEN-Akt axis promotes liver regeneration

Journal

ONCOTARGET
Volume 7, Issue 2, Pages 1584-1597

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.6444

Keywords

microRNA; liver regeneration; proliferation; PTEN; Akt

Funding

  1. National Natural Science Foundation of China [81400647, 81200169, 81370926, 81070343, 81370559, 81400635]
  2. Innovation Program of Shanghai Municipal Education Commission [13YZ014]
  3. Foundation for University Young Teachers by Shanghai Municipal Education Commission
  4. Shanghai University [sdcx2012038]
  5. Program for the integration of production, teaching and research for University Teachers - Shanghai Municipal Education Commission
  6. China Postdoctoral Science Foundation [2014M561456]
  7. Jonit Projects in Major Diseases from Shanghai Municipal Commission of Health and Family Planning [2014ZYJB0201]
  8. Jonit Projects for Novel Frontier Technology in Shanghai Municipal Hospital from Shanghai Municipal Commission of Health and Family Planning [SHDC1204122]
  9. Shanghai Medical Guide Project from Shanghai Science and Technology Committee [14411971500]
  10. Chinese Foundation for Hepatitis Prevention and Control [TQGB20140141]
  11. Shanghai Innovation Program [12431901002]

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Liver regeneration is a highly orchestrated process which can be regulated by microRNAs (miRNAs, miRs), though the mechanisms are largely unclear. This study was aimed to identify miRNAs responsible for hepatocyte proliferation during liver regeneration. Here we detected a marked elevation of miR-382 in the mouse liver at 48 hrs after partial hepatectomy (PH-48h) using microarray analysis and qRT-PCRs. miR-382 overexpression accelerated the proliferation and the G1 to S phase transition of the cell cycle both in mouse NCTC1469 and human HL7702 normal liver cells, while miR-382 downregulation had inverse effects. Moreover, miR-382 negatively regulated PTEN expression and increased Akt phosphorylation both in vitro and in vivo. Using PTEN siRNA and Akt activator/inhibitor, we further found that PTEN inhibition and Akt phosphorylation were essential for mediating the promotive effect of miR-382 in the proliferation and cell growth of hepatocytes. Collectively, our findings identify miR-382 as a promoter for hepatocyte proliferation and cell growth via targeting PTEN-Akt axis which might be a novel therapeutic target to enhance liver regeneration capability.

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